cDNA level identifier (n.a.):
c.8-51491_172-56018del
Gene level identifier:
g.232808_408989del
Archive identifier/Other designation:
deletion of exon 2
Reference, alternative allele:
G+176182, G
Genomic location hg(19)
6:162739814 (not available on ExAC)
Gene name:
Consequence:
structural variation includes copy number variants inversions and translocations
Pathogenicity scoring:
Definitely pathogenic
CADD score:
not available
Positive functional evidence:
not available
Number of all included cases:
1 compound heterozygous (1 in total).